Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → N-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-glycine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenic acid | HCID 128570 | — |
| 반응물 | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | N-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-glycine | HCID 54055783 | 85% |
반응 단계
The reaction of 6.1 g of 3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenoic acid with glycine ethyl ester hydrochloride was conducted in the same manner as described in Example 1 except that 6.5 ml of triethylamine was used. Then, a solution of 2.7 g of potassium hydroxide in ethanol was added. The mixture was heated under reflux for 30 minutes. After the completion of the reaction, water was added and the obtained aqueous solution was extracted with ethyl acetate. The ethyl acetate layer was washed with water and dried over magnesium sulfate. The solvent was distilled off to afford 6.1 g (yield 85%) of the title compound as a pale brown oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04762829 |
| 출처 데이터셋 | uspto-grants-1988_08 |
| ORD ID | ord-1d5e702110244a0e832fd0d8c9e22490 |
| 출처 메모 | uspto-grants-1988_08 |